Catalog

ASAP is committed to accelerating the pace of discovery and informing a path to a cure for Parkinson’s disease through collaboration, research-enabling resources, and data sharing. We’ve created this catalog to showcase the research outputs and tools developed by ASAP-funded programs.

Protocol

Mouse sample collection for metabolomics studies

Protocol used in the Mazmanian lab for collecting brain and gut tissues and plasma from mouse for metabolomics.

Protocol

Whole gut transit time, fecal water content, and fecal output

Protocol for mouse gastrointestinal function assays (whole gut transit time, fecal water content, and fecal output).

Protocol

Colonic migrating motor complexes

Protocol for ex vivo assay of colonic migrating motor complexes (CMMCs) in mouse colons.

Protocol

Quantitative targeted metabolomics for ASO mouse model using Biocrates Q500 platform

Protocol for using the Biocrates MxP-Q500 kit (BIOCRATES Life Science AG, Innsbruck, Austria), a commercially-available targeted metabolomics platform, to measure 634 metabolites across 26 biochemical classes from different tissues of the mouse.

Dataset

Data and code for “α-Synuclein Overexpression and the Microbiome Shape the Gut and Brain Metabolome in Mice”

Metabolomic data and analysis code associated with the article, “α-Synuclein Overexpression and the Microbiome Shape the Gut and Brain Metabolome in Mice.”

Article

α-Synuclein overexpression and the microbiome shape the gut and brain metabolome in mice

Pathological forms of α-synuclein contribute to Parkinson’s disease (PD). Most cases of PD are believed to arise from gene-environment interactions. Microbiome composition is altered in PD, and gut bacteria are causal to symptoms and pathology in animals. Here, the authors explore how the microbiome may impact PD-associated genetic risks.

Dataset

Fecal metagenomic sequencing data for PD patients and controls from Rush University Medical Center

Fecal metagenomic sequencing data associated with Boktor et al. (2023). This dataset includes samples from the Rush University Medical Center cohort.